Canonical Allele Identifier: CA1918977657

Gene: CHST3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.72009841_72009843delinsGTT , CM000672.2:g.72009841_72009843delinsGTT	GRCh38
NC_000010.10:g.73769599_73769601delinsGTT , CM000672.1:g.73769599_73769601delinsGTT	GRCh37
NC_000010.9:g.73439605_73439607delinsGTT	NCBI36
NG_012635.1:g.50480_50482delinsGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373115.5:c.*1370_*1372delinsGTT MANE Select	ENSP00000362207.4:n.*1370_*1372delinsGTT
ENST00000373115.4:c.*1370_*1372delinsGTT	ENSP00000362207.4:n.*1370_*1372delinsGTT
NM_004273.4:c.*1370_*1372delinsGTT	NP_004264.2:n.*1370_*1372delinsGTT
XM_006718075.2:c.*1370_*1372delinsGTT	XP_006718138.1:n.*1370_*1372delinsGTT
XM_011540369.1:c.*1370_*1372delinsGTT	XP_011538671.1:n.*1370_*1372delinsGTT
XM_006718075.4:c.*1370_*1372delinsGTT	XP_006718138.1:n.*1370_*1372delinsGTT
XM_011540369.2:c.*1370_*1372delinsGTT	XP_011538671.1:n.*1370_*1372delinsGTT
NM_004273.5:c.*1370_*1372delinsGTT MANE Select	NP_004264.2:n.*1370_*1372delinsGTT